4.6 Article

Reversely trapping atoms from a perovskite surface for high-performance and durable fuel cell cathodes

Journal

NATURE CATALYSIS
Volume 5, Issue 4, Pages 300-310

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41929-022-00764-9

Keywords

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Funding

  1. National Key R&D Program of China [2018YFA0702003]
  2. National Natural Science Foundation of China [21890383, 21871159, 22171157, 52002249]
  3. Beijing Natural Science Foundation [2214061]
  4. Science and Technology Key Project of Guangdong Province of China [2020B010188002]
  5. Guangdong Basic and Applied Basic Research Foundation [2019A1515110025]
  6. Fundamental Research Funds for the Central Universities [WUT: 2019III012GX, 2020III002GX]
  7. China Postdoctoral Science Foundation [2019M660607]
  8. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing (Wuhan University of Technology)
  9. State Key Laboratory of Silicate Materials for Architectures (Wuhan University of Technology)
  10. Shuimu Tsinghua Scholar Program

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This article investigates a reverse atom-trapping strategy to improve cathode performance in solid-oxide fuel cells by controlling the extraction of strontium atoms from the surface. The experimental results show that this strategy significantly increases the power density of single cells and improves the longevity of the cathode.
Atom trapping of scarce precious metals onto a suitable support at high temperatures has emerged as an effective approach to build thermally stable single-atom catalysts. Here, following a similar mechanism based on atom trapping through support effects, we demonstrate a reverse atom-trapping strategy to controllably extract strontium atoms from a rigid lanthanum strontium cobalt ferrite ((La0.6Sr0.4)(0.)95Co0.2Fe0.8O3-delta, LSCF) surface with ease. The lattice oxygen redox activity of LSCF is accordingly fine-tuned, leading to enhanced cathode performance in a solid-oxide fuel cell. An over 30-70% increases in maximum power density of the single cells at intermediate temperatures is achieved by LSCF with surface strontium vacancies compared to the pristine surface. In addition, the strontium-deficient surface excludes strontium segregation and formation of electrochemically inert SrO islands, thus improving the longevity of the cathode. This development can be broadly applicable for modifying structurally stable oxide surfaces, and opens more possibilities of scalable single-atom extraction strategies.

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